Canonical Allele Identifier: CA800603982

Gene: IDUA SLC26A1

Linked Data

• dbSNP Id: rs1237757080
• gnomAD v3: 4-987388-GGGT-G
• gnomAD v4: 4-987388-GGGT-G
• MyVariant Identifiers: chr4:g.981177_981179del (hg19) ; chr4:g.987389_987391del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.987391_987393del , CM000666.2:g.987391_987393del	GRCh38
NC_000004.11:g.981179_981181del , CM000666.1:g.981179_981181del	GRCh37
NC_000004.10:g.971179_971181del	NCBI36
NG_008103.1:g.5395_5397del
NG_033042.1:g.11046_11048del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.158+149_158+151del (IDUA)	ENSP00000247933.4:n.158+149_158+151del
ENST00000514224.2:c.158+149_158+151del (IDUA) MANE Select	ENSP00000425081.2:n.158+149_158+151del
ENST00000247933.8:c.158+149_158+151del (IDUA)	ENSP00000247933.4:n.158+149_158+151del
ENST00000398520.6:c.576+3737_576+3739del (SLC26A1)	ENSP00000381532.2:n.576+3737_576+3739del
ENST00000502910.5:c.158+149_158+151del (IDUA)	ENSP00000422952.1:n.158+149_158+151del
ENST00000504568.5:c.156+149_156+151del (IDUA)
ENST00000506561.5:n.167+149_167+151del (IDUA)
ENST00000508168.5:n.177+149_177+151del (IDUA)
ENST00000514698.5:n.199+149_199+151del (IDUA)
ENST00000622731.4:c.576+3737_576+3739del (SLC26A1)	ENSP00000483506.1:n.576+3737_576+3739del
NM_000203.4:c.158+149_158+151del (IDUA)	NP_000194.2:n.158+149_158+151del
NM_134425.2:c.576+3737_576+3739del (SLC26A1)	NP_602297.1:n.576+3737_576+3739del
NR_110313.1:n.246+149_246+151del (IDUA)
XM_011513459.1:c.158+149_158+151del (IDUA)	XP_011511761.1:n.158+149_158+151del
XM_011513460.1:c.158+149_158+151del (IDUA)	XP_011511762.1:n.158+149_158+151del
XR_924947.1:n.227+149_227+151del (IDUA)
NM_000203.5:c.158+149_158+151del (IDUA) MANE Select	NP_000194.2:n.158+149_158+151del
XM_017008163.1:c.-1309+149_-1309+151del (IDUA)	XP_016863652.1:n.-1309+149_-1309+151del
NM_134425.3:c.576+3737_576+3739del (SLC26A1)	NP_602297.1:n.576+3737_576+3739del
NM_134425.4:c.576+3737_576+3739del (SLC26A1)	NP_602297.1:n.576+3737_576+3739del